Application of mbl in the preparation of drugs for preventing or treating effector T-cell-induced diseases
A cell and drug technology, applied to metabolic diseases, antibacterial drugs, drug combinations, etc., to achieve the effect of rich sources and strong regenerative ability
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Embodiment 1
[0031] Experimental Materials
[0032] 1. The source of cells used in the experiment
[0033] Neonatal umbilical cord blood was collected from the Third Affiliated Hospital of Xinxiang Medical College and the Department of Obstetrics and Gynecology of Xinxiang First People's Hospital of full-term healthy newborns. Immediately after the fetus was delivered, blood was collected from the umbilical vein of the placenta and placed in a blood collection bag containing 28 mL of preservation solution. All blood samples were delivered to the laboratory within 4 hours after sampling.
[0034] 2. Main reagents
[0035] Medium RPMI1640, fetal bovine serum (FBS), and 10×PBS solution were all purchased from Thermo Fisher Scientific.
[0036] Lymphocyte separation medium (Ficoll-Paque PLUS), which is a sterile endotoxin (<0.12EU / mL) test solution of FicollTMPM400 and sodium diatrizoate with a density of 1.077g / mL, was purchased from GE Healthcare Life Sciences.
[0037] Anti-human CD3 mon...
Embodiment 2
[0094] Experimental Materials
[0095] 1. The source of cells used in the experiment
[0096] Reference example 1
[0097] 2. Main reagents
[0098] Reference example 1
[0099] 3. Main instruments and equipment
[0100] Reference example 1
[0101] 4. Preparation of common reagents
[0102] Reference example 1
[0103] experimental method
[0104] 1. Preparation of umbilical cord blood mononuclear cells
[0105] Reference example 1
[0106] 2. Coated with anti-CD3mAb
[0107] Reference example 1
[0108] 3. Magnetic separation of CD4+CD25-T cells and CD4+CD25+T cells
[0109] sample preparation
[0110] Peripheral mononuclear cells were separated by density gradient centrifugation. To remove platelets, cells were resuspended in buffer and centrifuged at 200×g for 10-15 min. The supernatant was carefully aspirated and washed repeatedly.
[0111] Magnetic labeling of non-CD4+ T cells
[0112] The whole process should be completed quickly, and the cells should be k...
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